rs35744605

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs35744605(G;T)

Make rs35744605(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

162277580

Gene

IFIH1

is a	snp
is	mentioned by
dbSNP	rs35744605
dbSNP (classic)	rs35744605
ClinGen	rs35744605
ebi	rs35744605
HLI	rs35744605
Exac	rs35744605
Gnomad	rs35744605
Varsome	rs35744605
LitVar	rs35744605
Map	rs35744605
PheGenI	rs35744605
Biobank	rs35744605
1000 genomes	rs35744605
hgdp	rs35744605
ensembl	rs35744605
geneview	rs35744605
scholar	rs35744605
google	rs35744605
pharmgkb	rs35744605
gwascentral	rs35744605
openSNP	rs35744605
23andMe	rs35744605
SNPshot	rs35744605
SNPdbe	rs35744605
MSV3d	rs35744605
GWAS Ctlg	rs35744605

GMAF

0.001837

Max Magnitude

0

[PMID 20736039] Loss-of-function mutations E6 27X and I923V of IFIH1 are associated with lower poly(I:C)-induced interferon-? production in peripheral blood mononuclear cells of type 1 diabetes patients

[PMID 22110759 ] Polymorphisms in the Innate Immune IFIH1 Gene, Frequency of Enterovirus in Monthly Fecal Samples during Infancy, and Islet Autoimmunity

[PMID 23144876 ] Enterovirus RNA in Peripheral Blood May Be Associated with the Variants of rs1990760, a Common Type 1 Diabetes Associated Polymorphism in IFIH1

ClinVar
Risk	rs35744605(A;A) rs35744605(C;C) rs35744605(T;T)
Alt	rs35744605(A;A) rs35744605(C;C) rs35744605(T;T)
Reference	Rs35744605(G;G)
Significance	Probable-non-pathogenic
Disease	not provided
Variation	info
Gene	IFIH1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.163134090C>A
CLNSRC
CLNACC	RCV000430296.1,